Thioether amide PC

Base Information

Chemical Name:Thioether amide PC
CAS No.:144000-46-4
Molecular Formula:C₂₀H₄₃N₂O₅PS
Molecular Weight:454.612
Hs Code.:
DSSTox Substance ID:DTXSID90932184
Mol file:144000-46-4.mol

Synonyms:1-(hexylthio)-2-(hexanoylamino)-1,2-dideoxy-sn-glycero-3-phosphocholine;1-palmitylthio-2-palmitoylamino-1,2-dideoxy-sn-glycero-3-phosphorylcholine;THIOAMID-PC;thioether amide PC;thioetheramide-PC

Suppliers and Price of Thioether amide PC

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 1 raw suppliers

Chemical Property of Thioether amide PC

Chemical Property:

PSA：126.29000
LogP:5.48330
XLogP3:3.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:19
Exact Mass:454.26303065
Heavy Atom Count:29
Complexity:466

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCSCC(COP(=O)([O-])OCC[N+](C)(C)C)NC(=O)CCCCC
Isomeric SMILES:CCCCCCSC[C@H](COP(=O)([O-])OCC[N+](C)(C)C)NC(=O)CCCCC

Technology Process of Thioether amide PC

There total 6 articles about Thioether amide PC which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 638-45-9
1-Iodohexane

: 144000-46-4
C₂₀H₄₃N₂O₅PS

Guidance literature:: Multi-step reaction with 6 steps

1: 8.5 g / sodium methoxide / methanol / Ambient temperature

2: pyridine / CHCl₃ / 4 h / Ambient temperature

3: aq. NaHCO₃ / CHCl₃ / 0.17 h

4: 71 percent / CHCl₃; propan-2-ol; dimethylformamide / 6 h / 50 °C

5: 99 percent / trifluoroacetic acid / 0.5 h / Ambient temperature

6: triethylamine / CHCl₃ / 24 h / Ambient temperature

With pyridine; sodium methylate; sodium hydrogencarbonate; triethylamine; trifluoroacetic acid; In methanol; chloroform; N,N-dimethyl-formamide; isopropyl alcohol;

Reference yield:

: 144000-38-4
1-(hexylthio)-2-(tritylamino)-1,2-dideoxy-sn-glycerol

: 144000-46-4
C₂₀H₄₃N₂O₅PS

Guidance literature:: Multi-step reaction with 5 steps

1: pyridine / CHCl₃ / 4 h / Ambient temperature

2: aq. NaHCO₃ / CHCl₃ / 0.17 h

3: 71 percent / CHCl₃; propan-2-ol; dimethylformamide / 6 h / 50 °C

4: 99 percent / trifluoroacetic acid / 0.5 h / Ambient temperature

5: triethylamine / CHCl₃ / 24 h / Ambient temperature

With pyridine; sodium hydrogencarbonate; triethylamine; trifluoroacetic acid; In chloroform; N,N-dimethyl-formamide; isopropyl alcohol;

Reference yield:

: 144000-39-5
1-(hexylthio)-2-(tritylamino)-1,2-dideoxy-3-((2'-bromoethyl)phospho)-sn-glycerol

: 144000-46-4
C₂₀H₄₃N₂O₅PS

Guidance literature:: Multi-step reaction with 3 steps

1: 71 percent / CHCl₃; propan-2-ol; dimethylformamide / 6 h / 50 °C

2: 99 percent / trifluoroacetic acid / 0.5 h / Ambient temperature

3: triethylamine / CHCl₃ / 24 h / Ambient temperature

With triethylamine; trifluoroacetic acid; In chloroform; N,N-dimethyl-formamide; isopropyl alcohol;